Canonical Allele Identifier: CA2147070159
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493585G= , CM000676.2:g.74493585G= GRCh38
NC_000014.8:g.74960288G= , CM000676.1:g.74960288G= GRCh37
NC_000014.7:g.74030041G= NCBI36
NG_007117.1:g.4797C=
NG_033074.1:g.4866G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-79C= ENSP00000450887.1:n.-79C=
ENST00000556009.5:c.147+446C=